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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818261Generated: October 30, 2026

2-Aminothiazole → 1,1-Dicyclohexyl-3-thiazol-2-yl-urea

https://huagongshe.com/reaction/1818261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantDicyclohexylamineHCID 7582—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1,1-Dicyclohexyl-3-thiazol-2-yl-ureaHCID 11174284—

Reaction Steps

To a solution of aminothiazole (50 mg, 0.5 mmol) in dichloromethane was added carbonyldiimidazole (81 mg, 0.5 mmol) and the solution stirred 2 h at room temperature. Dicyclohexylamine (1 eq) was then added and the reaction stirred overnight at room temperature. The reaction mixture is then diluted with ethyl acetate (8 mL), washed successively with 10% sodiumhydrogensulphate (3 mL), water (3 mL), dried over magnesium sulphate, concentrated in vacuo, and the residue purified by HPLC (Gilson 1, X-terra column; 0-100% CH3CN/H2O/0.1% TFA; 15 min; flow 50 ml/min) to give the title product (52 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598391B2
Source datasetuspto-grants-2009_10
ORD IDord-7c29f0b2d53947babee00913dae264dc
Source noteuspto-grants-2009_10